首页> 美国卫生研究院文献>International Journal for Parasitology: Drugs and Drug Resistance >Assessment of Draxxin® (tulathromycin) as an inhibitor of in vitro growth of Babesia bovis Babesia bigemina and Theileria equi
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Assessment of Draxxin® (tulathromycin) as an inhibitor of in vitro growth of Babesia bovis Babesia bigemina and Theileria equi

机译:评估Draxxin®(图拉霉素)作为牛肝杆菌双歧杆菌和马鞭毛虫的体外生长抑制剂

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摘要

Babesia bovis, Babesia bigemina and Theileria equi are worldwide tick-borne hemoprotozoan that cause diseases characterized by fever, anemia, weight loss and abortion. A common feature of these diseases are transition from acute to chronic phases, in which parasites may persist in the host for life, and becoming a reservoir for tick transmission. The live-attenuated vaccines for B. bovis and B. bigemina are not available for worldwide use due to legal restrictions and other concerns such as potential erythrocyte antigen and pathogen contamination, and a vaccine for T. equi is not available. The use of chemotherapeutics is essential to treat and control these diseases, but several studies have shown the development of drug-resistance by these parasites, and safe and effective alternative drugs are needed. Tulathromycin, a macrolide antibiotic, has proven to be effective against a vast range of bacteria and Plasmodium yoelli, a Babesia and Theileria related intra-erythrocytic apicomplexan. Draxxin® (tulathromycin) is currently licensed to treat infections that cause respiratory diseases in cattle in several countries. In this study, the activity of Draxxin® was tested in vitro on cultured B. bovis, B. bigemina and T. equi. Addition of the drug to in vitro cultures resulted in cessation of parasite replication of the three species tested, B. bovis, B. bigemina and T. equi, with estimated IC50 of 16.7 ± 0.6 nM; 6.2 ± 0.2 nM and 2.4 ± 0.1 nM, respectively, at 72 h. Furthermore, neither parasites nor parasite DNA were detectable in cultures treated with IC100, suggesting Draxxin® is a highly effective anti-Babesia/Theileria drug. Importantly, the IC50 calculated for Draxxin® for the Babesia/Theileria parasites tested is lower that the IC50 calculated for some drugs currently in use to control these parasites. Collectively, the data strongly support in vivo testing of Draxxin® for the treatment of bovine babesiosis and equine piroplasmosis.
机译:牛肝杆菌,大巴贝虫和马鞭毛虫是世界范围内的tick传播血原虫,会引起以发热,贫血,体重减轻和流产为特征的疾病。这些疾病的共同特征是从急性期过渡到慢性期,其中寄生虫可能在宿主体内终生存在,并成为壁虱传播的宿主。由于法律限制和其他方面的考虑,例如潜在的红细胞抗原和病原体污染,针对牛双歧杆菌和双歧双歧杆菌的减毒活疫苗无法在全球范围内使用,也没有针对马链球菌的疫苗。化学疗法的使用对于治疗和控制这些疾病至关重要,但是一些研究表明这些寄生虫会产生耐药性,因此需要安全有效的替代药物。已证明大环内酯类抗生素图拉霉素对多种细菌和约贝氏疟原虫和泰勒氏菌相关的红细胞内apicomplexan均有效。目前,Draxxin ®(图拉霉素)已获​​许可用于治疗在一些国家的牛中引起呼吸道疾病的感染。在这项研究中,Draxxin ®的活性在体外对培养的牛双歧杆菌,双歧杆菌和马鞭毛虫进行了测试。将药物添加到体外培养物中导致停止了所测试的三个物种的牛血清白僵菌,大双歧杆菌和马齿T的寄生虫复制,估计IC50为16.7±0.6±nM。在72 h时分别为6.2±0.2 nM和2.4±0.1 nM。此外,用IC100处理的培养物中均未检出寄生虫或寄生虫DNA,这表明Draxxin ®是一种高效的抗巴贝斯虫/泰勒虫药。重要的是,对于测试的贝贝虫/泰勒虫寄生虫,Draxxin ®计算的IC50低于当前用于控制这些寄生虫的某些药物的IC50。总体而言,这些数据有力地支持了Draxxin ®的体内测试,用于治疗牛杆状杆菌病和马兜铃虫病。

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